Magnesium hydroxide and mineral oil emulsion is a combination of magnesium hydroxide that is used as an antacid and osmotic laxative and mineral oil that acts as a lubricant and emulsifying agent.
Uses:
-
Occasional constipation:
- It is used for the short-term treatment of occasional constipation.
Magnesium hydroxide and mineral oil emulsion Dose in Adults:
Dose as Laxative:
- OTC labeling: Oral: 45 to 60 mL at bedtime
Magnesium hydroxide and mineral oil emulsion Dose in Childrens:
Dose as Laxative: OTC labeling: Oral:
-
Children 6 years of age or less:
- Avoid using the drug.
-
Children 6 to 11 years:
- 20 to 30 mL at bedtime
-
Children 12 years of age or older:
- Refer to adult dosing.
Use during pregnancy:
- See individual agents (magnesium hydroxide and mineral oil).
Use during breastfeeding:
- See individual agents (magnesium hydroxide and mineral oil).
Dose in Kidney Disease:
- Patients with a reduced kidney function should take magnesium containing supplements or medications with caution.
- The risk of magneisum toxicity is higher especially if the CrCl is 30 ml/minute or less.
- Frequent monitoring of magnesium levels in these patients is essential.
Dose in Liver disease:
No dosage adjustment mentioned in patients with liver disease.
Side effects:
See individual agents for detailed side effects:
- Magnesium hydroxide
- Mineral oil
Contraindications:
Allergy reactions to magnesium hydroxide or mineral oil or any other component of the formulation
Warnings and precautions
-
Renal impairment
- Patients with severe renal impairment should not take magnesium supplements or magnesium-containing medications, especially if the daily doses are greater than 50 mEq.
- Patients may become ill from a decreased magnesium clearance.
- Magnesium toxicity can be more common if the CrCl level is below 30 ml/minute.
Magnesium hydroxide and mineral oil emulsion: Drug Interaction
Amphetamines |
Antacids may decrease the excretion of Amphetamines. |
Antipsychotic Agents (Phenothiazines) |
Antacids may decrease the absorption of Antipsychotic Agents (Phenothiazines). |
Bromperidol |
|
Calcium Channel Blockers |
May enhance the adverse/toxic effect of Magnesium Salts. Magnesium Salts may enhance the hypotensive effect of Calcium Channel Blockers. |
Captopril |
Antacids may decrease the serum concentration of Captopril. |
Cefpodoxime |
Antacids may decrease the serum concentration of Cefpodoxime. |
Cysteamine (Systemic) |
Antacids may diminish the therapeutic effect of Cysteamine (Systemic). |
Dexmethylphenidate |
Antacids may increase the absorption of Dexmethylphenidate. Specifically, antacids may interfere with the normal release of drug from the extended-release capsules (Focalin XR brand), which could result in both increased absorption (early) and decreased delayed absorption. |
Diacerein |
Antacids may decrease the absorption of Diacerein. |
Dichlorphenamide |
Laxatives may enhance the hypokalemic effect of Dichlorphenamide. |
Methylphenidate |
Antacids may increase the absorption of Methylphenidate. Specifically, antacids may interfere with the normal release of drug from the extended-release capsules (Ritalin LA brand), which could result in both increased absorption (early) and decreased delayed absorption. |
Neuromuscular-Blocking Agents |
Magnesium Salts may enhance the neuromuscular-blocking effect of Neuromuscular-Blocking Agents. |
Phytonadione |
Mineral Oil may decrease the serum concentration of Phytonadione. Specifically, mineral oil may decrease the absorption of phytonadione. |
QuiNIDine |
Antacids may decrease the excretion of QuiNIDine. |
Rosuvastatin |
Antacids may decrease the serum concentration of Rosuvastatin. |
Risk Factor D (Consider therapy modification) |
|
Acalabrutinib |
Antacids may decrease the serum concentration of Acalabrutinib. Management: Separate administration of acalabrutinib from the administration of any antacids by at least 2 hours in order to minimize the potential for a significant interaction. |
Alfacalcidol |
May increase the serum concentration of Magnesium Salts. |
Allopurinol |
Antacids may decrease the absorption of Allopurinol. |
Alpha-Lipoic Acid |
Magnesium Salts may decrease the absorption of Alpha-Lipoic Acid. AlphaLipoic Acid may decrease the absorption of Magnesium Salts. |
Atazanavir |
Antacids may decrease the absorption of Atazanavir. |
Bictegravir |
|
Bisacodyl |
Antacids may diminish the therapeutic effect of Bisacodyl. Antacids may cause the delayed-release bisacodyl tablets to release drug prior to reaching the large intestine. Gastric irritation and/or cramps may occur. |
Bismuth Subcitrate |
Antacids may diminish the therapeutic effect of Bismuth Subcitrate. Management: Avoid administration of antacids within 30 minutes of bismuth subcitrate (tripotassium bismuth dicitrate) administration. |
Bisphosphonate Derivatives |
Polyvalent Cation Containing Products may decrease the serum concentration of Bisphosphonate Derivatives. Management: Avoid administration of oral medications containing polyvalent cations within: 2 hours before or after tiludronate/clodronate/etidronate; 60 minutes after oral ibandronate; or 30 minutes after alendronate/risedronate. Exceptions: Pamidronate; Zoledronic Acid. |
Bosutinib |
Antacids may decrease the serum concentration of Bosutinib. Management: Administer antacids more than 2 hours before or after bosutinib. |
Calcitriol (Systemic) |
May increase the serum concentration of Magnesium Salts. Management: Consider using a non-magnesium-containing antacid or phosphate-binding product in patients also receiving calcitriol. If magnesium-containing products must be used with calcitriol, serum magnesium concentrations should be monitored closely. |
Cefditoren |
Antacids may decrease the serum concentration of Cefditoren. Management: Concomitant use of cefditoren with antacids is not recommended. Consider alternative methods to control acid reflux (eg, diet modification) or alternative antimicrobial therapy. If antacid therapy can not be avoided, separate dosing by several hours. |
Cefuroxime |
Antacids may decrease the serum concentration of Cefuroxime. Management: Administer cefuroxime axetil at least 1 hour before or 2 hours after the administration of shortacting antacids. |
Chloroquine |
Antacids may decrease the serum concentration of Chloroquine. Management: Separate administration of antacids and chloroquine by at least 4 hours to minimize any potential negative impact of antacids on chloroquine bioavailability. |
Corticosteroids (Oral) |
Antacids may decrease the bioavailability of Corticosteroids (Oral). Management: Consider separating doses by 2 or more hours. Budesonide enteric coated tablets could dissolve prematurely if given with drugs that lower gastric acid, with unknown impact on budesonide therapeutic effects. |
Dabigatran Etexilate |
Antacids may decrease the serum concentration of Dabigatran Etexilate. Management: Dabigatran etexilate Canadian product labeling recommends avoiding concomitant use with antacids for 24 hours after surgery. In other situations, administer dabigatran etexilate 2 hours prior to antacids. Monitor clinical response to dabigatran therapy. |
Dasatinib |
Antacids may decrease the serum concentration of Dasatinib. Management: Simultaneous administration of dasatinib and antacids should be avoided. Administer antacids 2 hours before or 2 hours after dasatinib. |
Deferiprone |
Polyvalent Cation Containing Products may decrease the serum concentration of Deferiprone. Management: Separate administration of deferiprone and oral medications or supplements that contain polyvalent cations by at least 4 hours. |
Delavirdine |
Antacids may decrease the serum concentration of Delavirdine. Management: Separate doses of delavirdine and antacids by at least 1 hour. Monitor for decreased delavirdine therapeutic effects with this combination. |
Dolutegravir |
Magnesium Salts may decrease the serum concentration of Dolutegravir. Management: Administer dolutegravir at least 2 hours before or 6 hours after oral magnesium salts. Administer the dolutegravir/rilpivirine combination product at least 4 hours before or 6 hours after oral magnesium salts. |
Doxercalciferol |
May enhance the hypermagnesemic effect of Magnesium Salts. Management: Consider using a non-magnesium-containing antacid or phosphate-binding product in patients also receiving doxercalciferol. If magnesium-containing products must be used with doxercalciferol, serum magnesium concentrations should be monitored closely. |
Eltrombopag |
Polyvalent Cation Containing Products may decrease the serum concentration of Eltrombopag. Management: Administer eltrombopag at least 2 hours before or 4 hours after oral administration of any polyvalent cation containing product. |
Elvitegravir |
Antacids may decrease the serum concentration of Elvitegravir. Management: Separate administration of antacids and elvitegravir-containing products by at least 2 hours in order to minimize the risk for an interaction. |
Erdafitinib |
Serum Phosphate Level-Altering Agents may diminish the therapeutic effect of Erdafitinib. Management: Avoid coadministration of serum phosphate level-altering agents with erdafitinib before initial dose increase period based on serum phosphate levels (Days 14 to 21). |
Erlotinib |
Antacids may decrease the serum concentration of Erlotinib. Management: Separate the administration of erlotinib and any antacid by several hours in order to minimize the risk of a significant interaction. |
Fexofenadine |
Antacids may decrease the serum concentration of Fexofenadine. Management: Separate the administration of fexofenadine and aluminum- or magnesium-containing antacids. |
Fosinopril |
Antacids may decrease the serum concentration of Fosinopril. Management: The US and Canadian fosinopril manufacturer labels recommend separating the doses of antacids and fosinopril by 2 hours. |
Gabapentin |
Magnesium Salts may enhance the CNS depressant effect of Gabapentin. Specifically, high dose intravenous/epidural magnesium sulfate may enhance the CNS depressant effects of gabapentin. Magnesium Salts may decrease the serum concentration of Gabapentin. Management: Administer gabapentin at least 2 hours after use of a magnesiumcontaining antacid. Monitor patients closely for evidence of reduced response to gabapentin therapy. Monitor for CNS depression if high dose IV/epidural magnesium sulfate is used. |
Gefitinib |
Antacids may decrease the serum concentration of Gefitinib. Management: Administer gefitinib at least 6 hours before or after administration of an antacid, and closely monitor clinical response to gefitinib. |
Hyoscyamine |
Antacids may decrease the serum concentration of Hyoscyamine. Management: Administer immediate release hyoscyamine before meals and antacids after meals when these agents are given in combination. |
Iron Preparations |
Antacids may decrease the absorption of Iron Preparations. Management: Separate dosing of oral iron preparations and antacids as much as possible to avoid decreased efficacy of iron preparation. If coadministered with antacids, monitor for decreased therapeutic effects of iron preparations. Exceptions: Ferric Carboxymaltose; Ferric Citrate; Ferric Gluconate; Ferric Hydroxide Polymaltose Complex; Ferric Pyrophosphate Citrate; Ferumoxytol; Iron Dextran Complex; Iron Isomaltoside; Iron Sucrose. |
Itraconazole |
Antacids may decrease the serum concentration of Itraconazole. Antacids may increase the serum concentration of Itraconazole. Management: Administer Sporanox brand itraconazole at least 2 hours before or 2 hours after administration of any antacids. Exposure to Tolsura brand itraconazole may be increased by antacids; consider itraconazole dose reduction. |
Ketoconazole (Systemic) |
Antacids may decrease the serum concentration of Ketoconazole (Systemic). Management: Administer oral ketoconazole at least 2 hours prior to use of any antacid product. Monitor patients closely for signs of inadequate clinical response to ketoconazole. |
Lanthanum |
Antacids may diminish the therapeutic effect of Lanthanum. |
Ledipasvir |
Antacids may decrease the serum concentration of Ledipasvir. Management: Separate the administration of ledipasvir and antacids by 4 hours. |
Levothyroxine |
Magnesium Salts may decrease the serum concentration of Levothyroxine. Management: Separate administration of oral levothyroxine and oral magnesium salts by at least 4 hours. |
Mesalamine |
Antacids may diminish the therapeutic effect of Mesalamine. Antacid-mediated increases in gastrointestinal pH may cause the premature release of mesalamine from specific sustained-release mesalamine products. Management: Avoid concurrent administration of antacids with sustained-release mesalamine products. Separating antacid and mesalamine administration, and/or using lower antacid doses may be adequate means of avoiding this interaction. |
Methenamine |
Antacids may diminish the therapeutic effect of Methenamine. |
Multivitamins/Fluoride (with ADE) |
Mineral Oil may decrease the serum concentration of Multivitamins/Fluoride (with ADE). Management: Avoid concomitant oral administration of mineral oil and multivitamins when possible; consider separating the administration of these agents by several hours to minimize the risk of interaction. |
Multivitamins/Minerals (with ADEK, Folate, Iron) |
Mineral Oil may decrease the serum concentration of Multivitamins/Minerals (with ADEK, Folate, Iron). Specifically, mineral oil may impair the absorption of fat-soluble vitamins. Management: Avoid concomitant oral administration of mineral oil and multivitamins when possible; consider separating the administration of these agents by several hours to minimize the risk of interaction. |
Multivitamins/Minerals (with AE, No Iron) |
Mineral Oil may decrease the serum concentration of Multivitamins/Minerals (with AE, No Iron). Management: Avoid concomitant oral administration of mineral oil and multivitamins when possible; consider separating the administration of these agents by several hours to minimize the risk of interaction. |
Mycophenolate |
Antacids may decrease the absorption of Mycophenolate. Management: Separate doses of mycophenolate and antacids by at least 2 hours. Monitor for reduced effects of mycophenolate if taken concomitant with antacids. |
Mycophenolate |
Magnesium Salts may decrease the serum concentration of Mycophenolate. Management: Separate doses of mycophenolate and oral magnesium salts. Monitor for reduced effects of mycophenolate if taken concomitant with oral magnesium salts. |
Neratinib |
Antacids may decrease the serum concentration of Neratinib. Specifically, antacids may reduce neratinib absorption. Management: Separate the administration of neratinib and antacids by giving neratinib at least 3 hours after the antacid. |
Nilotinib |
Antacids may decrease the serum concentration of Nilotinib. Management: Separate the administration of nilotinib and any antacid by at least 2 hours whenever possible in order to minimize the risk of a significant interaction. |
PAZOPanib |
Antacids may decrease the serum concentration of PAZOPanib. Management: Avoid the use of antacids in combination with pazopanib whenever possible. Separate doses by several hours if antacid treatment is considered necessary. The impact of dose separation has not been investigated. |
PenicillAMINE |
Polyvalent Cation Containing Products may decrease the serum concentration of PenicillAMINE. Management: Separate the administration of penicillamine and oral polyvalent cation containing products by at least 1 hour. |
Pexidartinib |
Antacids may decrease the serum concentration of Pexidartinib. Management: Administer pexidartinib 2 hours before or after antacids. |
Phosphate Supplements |
Antacids may decrease the absorption of Phosphate Supplements. Management: This applies only to oral phosphate administration. Separating administer of oral phosphate supplements from antacid administration by as long as possible may minimize the interaction. Exceptions: Sodium Glycerophosphate Pentahydrate. |
Phosphate Supplements |
Magnesium Salts may decrease the serum concentration of Phosphate Supplements. Management: Administer oral phosphate supplements as far apart from the administration of an oral magnesium salt as possible to minimize the significance of this interaction. Exceptions: Sodium Glycerophosphate Pentahydrate. |
Potassium Phosphate |
Antacids may decrease the serum concentration of Potassium Phosphate. Management: Consider separating administration of antacids and oral potassium phosphate by at least 2 hours to decrease risk of a significant interaction. |
Quinolones |
Antacids may decrease the absorption of Quinolones. Of concern only with oral administration of quinolones. Management: Avoid concurrent administration of quinolones and antacids to minimize the impact of this interaction. Recommendations for optimal dose separation vary by specific quinolone. Exceptions: LevoFLOXacin (Oral Inhalation). |
Quinolones |
Magnesium Salts may decrease the serum concentration of Quinolones. Management: Administer oral quinolones several hours before (4 h for moxi/pe/spar-, 2 h for others) or after (8 h for moxi-, 6 h for cipro/dela-, 4 h for lome/pe-, 3 h for gemi-, and 2 h for levo-, nor-, or ofloxacin or nalidixic acid) oral magnesium salts. Exceptions: LevoFLOXacin (Oral Inhalation). |
Rilpivirine |
Antacids may decrease the serum concentration of Rilpivirine. Management: Administer antacids at least 2 hours before or 4 hours after rilpivirine. Administer antacids at least 6 hours before or 4 hours after the rilpivirine/dolutegravir combination product. |
Riociguat |
Antacids may decrease the serum concentration of Riociguat. Management: Separate the administration of antacids and riociguat by at least 1 hour in order to minimize any potential interaction. |
Sotalol |
Antacids may decrease the serum concentration of Sotalol. Management: Avoid simultaneous administration of sotalol and antacids. Administer antacids 2 hours after sotalol. |
Strontium Ranelate |
Magnesium Hydroxide may decrease the serum concentration of Strontium Ranelate. Management: Separate administration of strontium ranelate and magnesium hydroxide by at least 2 hours whenever possible in order to minimize this interaction. |
Sulpiride |
Antacids may decrease the serum concentration of Sulpiride. Management: Separate administration of antacids and sulpiride by at least 2 hours in order to minimize the impact of antacids on sulpiride absorption. |
Tetracyclines |
Antacids may decrease the absorption of Tetracyclines. Management: Separate administration of antacids and oral tetracycline derivatives by several hours when possible to minimize the extent of this potential interaction. Exceptions: Eravacycline. |
Tetracyclines |
Magnesium Salts may decrease the absorption of Tetracyclines. Only applicable to oral preparations of each agent. Exceptions: Eravacycline. |
Trientine |
Polyvalent Cation Containing Products may decrease the serum concentration of Trientine. Management: Avoid concomitant administration of trientine and oral products that contain polyvalent cations. If oral iron supplements are required, separate the administration by 2 hours. If other oral polyvalent cations are needed, separate administration by 1 hour. |
Velpatasvir |
Antacids may decrease the serum concentration of Velpatasvir. Management: Separate administration of velpatasvir and antacids by at least 4 hours. |
Vitamin D Analogs |
Mineral Oil may decrease the serum concentration of Vitamin D Analogs. More specifically, mineral oil may interfere with the absorption of Vitamin D Analogs. Management: Avoid concomitant, oral administration of mineral oil and vitamin D analogs. Consider separating the administration of these agents by several hours to minimize the risk of interaction. Monitor plasma calcium concentrations. Exceptions: Calcipotriene; Calcitriol (Topical); Tacalcitol. |
Risk Factor X (Avoid combination) |
|
Baloxavir Marboxil |
Polyvalent Cation Containing Products may decrease the serum concentration of Baloxavir Marboxil. |
Calcium Polystyrene Sulfonate |
Laxatives (Magnesium Containing) may enhance the adverse/toxic effect of Calcium Polystyrene Sulfonate. More specifically, concomitant use of calcium polystyrene sulfonate with magnesium-containing laxatives may result in metabolic alkalosis or with sorbitol may result in intestinal necrosis. Management: Avoid concomitant use of calcium polystyrene sulfonate (rectal or oral) and magnesium-containing laxatives. |
MiSOPROStol |
Antacids may enhance the adverse/toxic effect of MiSOPROStol. More specifically, concomitant use with magnesium-containing antacids may increase the risk of diarrhea. Management: Avoid concomitant use of misoprostol and magnesium-containing antacids. In patients requiring antacid therapy, employ magnesium-free preparations. Monitor for increased adverse effects (e.g., diarrhea, dehydration). |
QuiNINE |
Antacids may decrease the serum concentration of QuiNINE. |
Raltegravir |
Magnesium Salts may decrease the serum concentration of Raltegravir. Management: Avoid the use of oral / enteral magnesium salts with raltegravir. No dose separation schedule has been established that adequately reduces the magnitude of interaction. |
Sodium Polystyrene Sulfonate |
Laxatives (Magnesium Containing) may enhance the adverse/toxic effect of Sodium Polystyrene Sulfonate. More specifically, concomitant use of sodium polystyrene sulfonate with magnesium-containing laxatives may result in metabolic alkalosis or with sorbitol may result in intestinal necrosis. Management: Avoid concomitant use of sodium polystyrene sulfonate (rectal or oral) and magnesium-containing laxatives. |
Monitoring Parameters:
None mentioned. If the patient develops severe diarrhea, monitor hydration status and serum electrolytes.
How to administer Magnesium hydroxide and mineral oil emulsion?
Before using the suspension, shake it well and administer followed by a glass of liquid or water. Avoid taking it with meals.
Mechanism of action:
- Mineral oil is used to lubricate and emulsify the oil.
- Magnesium hydroxide acts to draw in water to the intestines to relieve constipation.
- It can be used as a laxative, with a duration of 30 minutes to 6 hour hours.
Excretion
- Approximately 30% of systemically absorbed magnesium is excreted through the urine. The unabsorbed drug is expelled via the feces.
International Brands Names:
- Phillips'® M-O
Brand Names in Pakistan:
No Brands Available in Pakistan.